RS138307707 SLC17A8

Health Risk Chr 12:100404103 snv missense variant

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Associated Conditions

Autosomal dominant nonsyndromic hearing loss 25

SLC17A8-related disorder

Autosomal dominant nonsyndromic hearing loss 25

SLC17A8-related disorder

Population Frequencies

gnomAD ALL

100%

1kG AFR

100%

1kG ALL

99.8%

1kG AMR

100%

1kG EAS

99.1%

1kG EUR

99.9%

1kG SAS

99.9%

Other Variants in SLC17A8